Data / Medical devices / United States / Dynapulse Medical LLC
Dynapulse Medical LLC: FDA-registered device maker in Minnetonka, MN, United States, 3 510(k) clearances
Dynapulse Medical LLC is registered with the FDA (registration 3027718340) in Minnetonka, MN, United States. It lists 5 device types. The FDA files 3 510(k) clearances under its listings, the newest dated December 23, 2025. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3027718340
- Address
- 13500 Wayzata Blvd., Minnetonka, MN, United States, 55305
- Owner or operator
- DynaPulse Medical LLC (10088485)
- Roles
- Specification developer
- First device listed
- January 22, 2025
- Registered through
- 2027
- Brand names listed
- Veinoplus
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Specification developer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Specification developer | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Specification developer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Specification developer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 23, 2025 | K251958 | VEINOPLUS Back | NUH | Substantially Equivalent | Dynapulse Medical | accessdata.fda.gov |
| June 16, 2015 | K141919 | VEINOPLUS SPORT NEUROMUSCULAR STIMULATOR | NGX | Substantially Equivalent | Ad Rem Technology Sarl | accessdata.fda.gov |
| January 30, 2008 | K072252 | VEINOPLUS NEUROMUSCULAR STIMULATOR | IPF | Substantially Equivalent | Ad Rem Technology Sarl | accessdata.fda.gov |
Compare with other makers
- All makers of Electrode, Cutaneous
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Stimulator, Muscle, Powered
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
Updated December 23, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.